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Identification of a familial cleidocranial dysplasia with a novel RUNX2 mutation and establishment of patient-derived induced pluripotent stem cells.
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- Odontology, 2022, v. 110, n. 3, p. 444, doi. 10.1007/s10266-021-00674-5
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- Article
Induction of Noonan syndrome-specific human-induced pluripotent stem cells under serum-, feeder-, and integration-free conditions.
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- In Vitro Cellular & Developmental Biology Animal, 2020, v. 56, n. 10, p. 888, doi. 10.1007/s11626-020-00515-9
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- Article
Induction of integration-free human-induced pluripotent stem cells under serum- and feeder-free conditions.
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- In Vitro Cellular & Developmental Biology Animal, 2020, v. 56, n. 1, p. 85, doi. 10.1007/s11626-019-00412-w
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- Article
Generation of cleidocranial dysplasia-specific human induced pluripotent stem cells in completely serum-, feeder-, and integration-free culture.
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- In Vitro Cellular & Developmental Biology Animal, 2016, v. 52, n. 2, p. 252, doi. 10.1007/s11626-015-9968-x
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- Article